5 years ago

Bifunctional Oxygen Electrocatalysis through Chemical Bonding of Transition Metal Chalcogenides on Conductive Carbons

Bifunctional Oxygen Electrocatalysis through Chemical Bonding of Transition Metal Chalcogenides on Conductive Carbons
Hyoyoung Lee, Doyoung Kim, Yongshin Kim, Anand P. Tiwari
Improving the electrochemical performance of both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) has been of great interest in emerging renewable energy technologies. This study reports an advanced bifunctional hybrid electrocatalyst for both ORR and OER, which is composed of tungsten disulphide (WS2) and carbon nanotube (CNT) connected via tungsten carbide (WC) bonding. WS2 sheets on the surface of CNTs provide catalytic active sites for electrocatalytic activity while the CNTs act as conduction channels and provide a large surface area. Moreover, the newly formed WC crystalline structure provides an easy path for electron transfer by spin coupling and helps to solve stability issues to enable excellent electrocatalytic activity. In addition, it is found that four to five layers of WS2 sheets on the surface of CNTs produce excellent catalytic activity toward both ORR and OER, which is comparable to noble metals (Pt, RuO2, etc.). These findings show the many advantages enabled by designing highly active, durable, and cost-effective ORR and OER electrocatalysts. An advanced bifunctional hybrid electrocatalyst is developed for both oxygen reduction reaction and oxygen evolution reaction, which is composed of tungsten disulphide (WS2) and carbon nanotube (CNT) connected via tungsten carbide bonding. WS2 sheets on the surface of CNTs provide catalytic active sites for electrocatalytic activity while the CNTs act as conduction channels and provide a large surface area.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/aenm.201602217

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.